Variant report

Variant	nsv1063556
Chromosome Location	chr19:20845947-20981129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:530)
CpG islands
(count:183)
Chromatin interactive
region (count:3)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:20958836-20959136	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:20847533-20847536	HepG2	liver:	n/a	n/a
3	ATF1	chr19:20958907-20959195	K562	blood:	n/a	n/a
4	BATF	chr19:20970646-20970943	GM12878	blood:	n/a	chr19:20970856-20970867 chr19:20970857-20970867
5	BATF	chr19:20933377-20933590	GM12878	blood:	n/a	n/a
6	BATF	chr19:20970637-20971050	GM12878	blood:	n/a	chr19:20970856-20970867 chr19:20970857-20970867
7	BATF	chr19:20847409-20847671	GM12878	blood:	n/a	n/a
8	BCL11A	chr19:20970637-20970914	GM12878	blood:	n/a	chr19:20970859-20970868 chr19:20970860-20970869
9	BHLHE40	chr19:20958960-20959285	GM12878	blood:	n/a	n/a
10	BRCA1	chr19:20959419-20959438	HepG2	liver:	n/a	n/a
11	BRCA1	chr19:20959318-20959498	GM12878	blood:	n/a	n/a
12	CEBPB	chr19:20848062-20848153	K562	blood:	n/a	n/a
13	CEBPB	chr19:20958824-20959032	K562	blood:	n/a	chr19:20959022-20959030
14	CEBPB	chr19:20847268-20847649	HepG2	liver:	n/a	chr19:20847466-20847477
15	CEBPB	chr19:20847966-20848184	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr19:20849035-20849295	K562	blood:	n/a	chr19:20849173-20849184
17	CEBPB	chr19:20847357-20847669	HepG2	liver:	n/a	chr19:20847466-20847477
18	CEBPB	chr19:20909924-20910145	HepG2	liver:	n/a	n/a
19	CEBPB	chr19:20849024-20849330	HepG2	liver:	n/a	chr19:20849173-20849184
20	CEBPB	chr19:20847896-20848234	HepG2	liver:	n/a	n/a
21	CEBPB	chr19:20847420-20847570	HepG2	liver:	n/a	chr19:20847466-20847477
22	CEBPB	chr19:20958915-20959172	HepG2	liver:	n/a	chr19:20959022-20959030
23	CEBPD	chr19:20847271-20847543	HepG2	liver:	n/a	n/a
24	CHD1	chr19:20959134-20959334	GM12878	blood:	n/a	n/a
25	CHD1	chr19:20959194-20959482	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr19:20959455-20959472	K562	blood:	n/a	n/a
27	CHD2	chr19:20958856-20959221	K562	blood:	n/a	n/a
28	CHD2	chr19:20958831-20959334	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr19:20958845-20959293	GM12878	blood:	n/a	n/a
30	CHD2	chr19:20958912-20959333	HepG2	liver:	n/a	n/a
31	CTCF	chr19:20933368-20933467	GM19238	blood:	n/a	n/a
32	CTCF	chr19:20970376-20970408	Lung_OC	lung:	n/a	n/a
33	CTCF	chr19:20933395-20933452	GM19240	blood:	n/a	n/a
34	CTCF	chr19:20959260-20959410	HepG2	liver:	n/a	n/a
35	CTCF	chr19:20897338-20897466	GM12878	blood:	n/a	chr19:20897423-20897444 chr19:20897424-20897432 chr19:20897421-20897434 chr19:20897421-20897439
36	CTCF	chr19:20952282-20952330	LNCaP	prostate:	n/a	n/a
37	CTCF	chr19:20933443-20933484	LNCaP	prostate:	n/a	n/a
38	CTCF	chr19:20934480-20934630	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr19:20959236-20959327	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr19:20947464-20947563	GM20000	blood:	n/a	n/a
41	CTCF	chr19:20943123-20943212	Lung_OC	lung:	n/a	n/a
42	CTCF	chr19:20931577-20931698	GM20000	blood:	n/a	n/a
43	CTCF	chr19:20959000-20959150	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr19:20934550-20934589	Medullo	brain:	n/a	n/a
45	CTCF	chr19:20893757-20893838	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr19:20932483-20932700	K562	blood:	n/a	n/a
47	CTCF	chr19:20913880-20913928	GM13976	blood:	n/a	n/a
48	CTCF	chr19:20941396-20941411	GM13976	blood:	n/a	n/a
49	CTCF	chr19:20883972-20883981	GM10248	blood:	n/a	n/a
50	CTCF	chr19:20954123-20954233	Lung_OC	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:20959492-20959542	HRCEpiC	kidney:	n/a
2	chr19:20959492-20959542	PANC-1	pancreas:	n/a
3	chr19:20959492-20959542	HCM	heart:	n/a
4	chr19:20959100-20959150	HMEC	breast:	n/a
5	chr19:20959100-20959150	LNCaP	prostate:	n/a
6	chr19:20959091-20959141	HRCEpiC	kidney:	n/a
7	chr19:20959492-20959542	AoSMC	blood vessel:	n/a
8	chr19:20959100-20959150	SK-N-SH_RA	brain:	n/a
9	chr19:20959091-20959141	NHBE	bronchial:	n/a
10	chr19:20959100-20959150	Caco-2	colon:	n/a
11	chr19:20959100-20959150	Hepatocyte	liver:	n/a
12	chr19:20959091-20959141	HIPEpiC	eye:	n/a
13	chr19:20959091-20959141	IMR90	lung:	fetal
14	chr19:20959100-20959150	HRCEpiC	kidney:	n/a
15	chr19:20959100-20959150	PANC-1	pancreas:	n/a
16	chr19:20959492-20959542	Jurkat	blood:	n/a
17	chr19:20959091-20959141	HMEC	breast:	n/a
18	chr19:20959091-20959141	RPTEC	kidney:	n/a
19	chr19:20959492-20959542	Hepatocyte	liver:	n/a
20	chr19:20959492-20959542	U87	brain:	n/a
21	chr19:20959492-20959542	AG09319	gingival:	n/a
22	chr19:20959100-20959150	GM19239	blood:	n/a
23	chr19:20959091-20959141	AG10803	skin:	n/a
24	chr19:20959100-20959150	HCT-116	colon:	n/a
25	chr19:20959492-20959542	ECC-1	luminal epithelium:	n/a
26	chr19:20959492-20959542	HMEC	breast:	n/a
27	chr19:20959091-20959141	HEK293	kidney:	embryo
28	chr19:20959091-20959141	GM12878	blood:	n/a
29	chr19:20959100-20959150	GM06990	blood:	n/a
30	chr19:20959091-20959141	GM19239	blood:	n/a
31	chr19:20959091-20959141	MCF-7	breast:	n/a
32	chr19:20959100-20959150	SK-N-SH	brain:	n/a
33	chr19:20959492-20959542	AG04450	lung:	fetal
34	chr19:20959492-20959542	HUVEC	blood vessel:	n/a
35	chr19:20959091-20959141	GM06990	blood:	n/a
36	chr19:20959492-20959542	HRE	kidney:	n/a
37	chr19:20959492-20959542	Hela-S3	cervix:	n/a
38	chr19:20959100-20959150	HAEpiC	amniotic membrane:	n/a
39	chr19:20959100-20959150	BE2_C	brain:	n/a
40	chr19:20959091-20959141	ProgFib	skin:	n/a
41	chr19:20959100-20959150	NT2-D1	testis:	n/a
42	chr19:20959100-20959150	HUVEC	blood vessel:	n/a
43	chr19:20959492-20959542	AG09309	skin:	n/a
44	chr19:20959091-20959141	HCPEpiC	choroid plexus:	n/a
45	chr19:20959100-20959150	HPAEpiC	pulmonary alveolar:	n/a
46	chr19:20959091-20959141	SK-N-SH	brain:	n/a
47	chr19:20959091-20959141	CMK	blood:	n/a
48	chr19:20959492-20959542	BJ	skin:	n/a
49	chr19:20959100-20959150	AG04449	skin:	fetal
50	chr19:20959100-20959150	NB4	blood:	n/a

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:20957022..20960457-chr19:20966415..20968798,3	K562	blood:
2	chr19:20957022..20960457-chr19:20966415..20968798,3	K562	blood:
3	chr19:20958957..20961587-chr19:20963643..20966546,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF85-3	chr19:20857719-20857891	XLOC_013004
2	lnc-ZNF85-8	chr19:20941246-20941758	NONHSAT063671
3	lnc-ZNF85-7	chr19:20946830-20947163	l_1659_chr19:20946829-20959081_testes
4	lnc-ZNF85-7	chr19:20957538-20959081	l_1659_chr19:20946829-20959081_testes
5	lnc-ZNF626-3	chr19:20967402-20967958	NONHSAT063672

No data

Variant related genes	Relation type
VN1R79P	TF binding region
ENSG00000269040	TF binding region
ZNF626	TF binding region
ENSG00000269110	TF binding region
ZNF66	TF binding region
ENSG00000268416	TF binding region
ENSG00000269779	TF binding region
VN1R79P	CpG island
ENSG00000269040	CpG island
ZNF626	CpG island
ENSG00000269110	CpG island
ZNF66	CpG island
ENSG00000268416	CpG island
ENSG00000269779	CpG island
ENSG00000160229	chromatin interactions
ENSG00000269040	chromatin interactions
WDR33	miRNA target sites

Extended variants
information (count: 2508 )
Associated
traits (count: 44 )

Variant overlapped rSNPs/rCNVs (count:2508 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs579161	chr19:20845971-20845972	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs535102897	chr19:20845978-20845979	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs555211578	chr19:20846003-20846004	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs575018332	chr19:20846026-20846027	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs553407350	chr19:20846054-20846055	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs7258695	chr19:20846111-20846112	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs577651565	chr19:20846139-20846140	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs540101867	chr19:20846143-20846144	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs577410215	chr19:20846168-20846169	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs140036331	chr19:20846214-20846215	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs573864085	chr19:20846263-20846264	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs4808260	chr19:20846271-20846272	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	disease
13	rs559887150	chr19:20846281-20846282	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs528464784	chr19:20846309-20846310	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs189676491	chr19:20846342-20846343	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs562145393	chr19:20846366-20846367	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs8108450	chr19:20846494-20846495	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs112259769	chr19:20846515-20846516	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs374771271	chr19:20846516-20846517	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs150115981	chr19:20846601-20846602	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs182757626	chr19:20846605-20846606	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs138375761	chr19:20846641-20846642	Weak transcription ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs113512000	chr19:20846727-20846728	Weak transcription ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs188076331	chr19:20846757-20846758	Weak transcription ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs656864	chr19:20846817-20846818	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs373148755	chr19:20846856-20846857	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs368888535	chr19:20846857-20846858	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs369581268	chr19:20846866-20846867	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs555043024	chr19:20846911-20846912	Weak transcription Enhancers ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs192725822	chr19:20846936-20846937	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs537337352	chr19:20846967-20846968	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs557646118	chr19:20846968-20846969	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs560694036	chr19:20847016-20847017	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs199511714	chr19:20847022-20847023	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs114930154	chr19:20847151-20847152	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs529614849	chr19:20847246-20847247	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs573357730	chr19:20847305-20847306	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs542370510	chr19:20847349-20847350	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs561932271	chr19:20847350-20847351	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs659147	chr19:20847351-20847352	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs550561362	chr19:20847387-20847388	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs183509795	chr19:20847397-20847398	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs562635118	chr19:20847444-20847445	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs11673057	chr19:20847449-20847450	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs566359560	chr19:20847460-20847461	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs560955950	chr19:20847469-20847470	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs138520560	chr19:20847480-20847481	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs187585674	chr19:20847534-20847535	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs192266907	chr19:20847550-20847551	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs537854057	chr19:20847564-20847565	Weak transcription Enhancers ZNF genes & repeats Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:44)

Disease	PMID	Source
Medulloblastoma	16783165	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Prostate cancer	16573809	CNVD
Chordoma	18071362	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
ovarian endometriomas	16273235	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Cervical cancer	21063398	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Lung cancer	18438408	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Colorectal cancer	20459617	CNVD
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1105 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:20844200-20847800	Weak transcription	Fetal Heart	heart
2	chr19:20844400-20847200	Weak transcription	Small Intestine	intestine
3	chr19:20844400-20847800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr19:20844400-20847800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr19:20844400-20847800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr19:20844400-20847800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr19:20844400-20847800	Weak transcription	Fetal Brain Male	brain
8	chr19:20844400-20847800	Weak transcription	Gastric	stomach
9	chr19:20844600-20847000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
10	chr19:20844600-20847600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr19:20844600-20847600	Weak transcription	Placenta	Placenta
12	chr19:20844600-20847600	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr19:20844600-20847600	Weak transcription	Stomach Smooth Muscle	stomach
14	chr19:20844600-20847800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr19:20844600-20847800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr19:20844600-20847800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr19:20844600-20847800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr19:20844600-20847800	Weak transcription	Brain Germinal Matrix	brain
19	chr19:20844600-20847800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr19:20844600-20847800	Weak transcription	Colonic Mucosa	Colon
21	chr19:20844600-20847800	Weak transcription	Fetal Lung	lung
22	chr19:20844600-20847800	Weak transcription	Ovary	ovary
23	chr19:20844600-20847800	Weak transcription	Rectal Smooth Muscle	rectum
24	chr19:20844600-20847800	Weak transcription	K562	blood
25	chr19:20844600-20848200	Weak transcription	Left Ventricle	heart
26	chr19:20844800-20846000	Enhancers	Brain Angular Gyrus	brain
27	chr19:20844800-20847400	Weak transcription	Adipose Nuclei	Adipose
28	chr19:20844800-20847600	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr19:20844800-20847800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr19:20844800-20847800	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr19:20844800-20847800	Weak transcription	Fetal Stomach	stomach
32	chr19:20844800-20848000	Weak transcription	Right Atrium	heart
33	chr19:20845000-20848800	ZNF genes & repeats	Fetal Intestine Small	intestine
34	chr19:20845200-20846000	Flanking Active TSS	HepG2	liver
35	chr19:20845200-20847000	Weak transcription	Primary B cells from peripheral blood	blood
36	chr19:20845200-20847000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr19:20845200-20847200	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr19:20845200-20847600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr19:20845600-20846000	Enhancers	Brain Substantia Nigra	brain
40	chr19:20845600-20847000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr19:20845600-20847200	Weak transcription	Brain Inferior Temporal Lobe	brain
42	chr19:20845600-20847200	Weak transcription	Pancreas	Pancrea
43	chr19:20845600-20847600	Weak transcription	Brain Hippocampus Middle	brain
44	chr19:20845600-20847800	Weak transcription	Brain Cingulate Gyrus	brain
45	chr19:20845800-20847400	Weak transcription	Skeletal Muscle Female	skeletal muscle
46	chr19:20845800-20847600	Weak transcription	Brain Anterior Caudate	brain
47	chr19:20846000-20847200	Weak transcription	Brain Substantia Nigra	brain
48	chr19:20846000-20847800	Weak transcription	Brain Angular Gyrus	brain
49	chr19:20846000-20848000	Active TSS	HepG2	liver
50	chr19:20846800-20848600	Enhancers	Fetal Intestine Large	intestine

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